Injector systems and syringe adapters for use therewith

ABSTRACT

An adapter includes a syringe carrier adapted to seat at least a portion of the syringe. The syringe carrier includes at least one rearward facing abutment member to abut at least one forward facing surface on a syringe. The syringe carrier includes an opening therein to allow a drive member of an injector to communicate forward force to the plunger through abutment without connective engagement between the drive member and the plunger. The adapter further includes a releasable mounting mechanism positioned to the rear of the syringe carrier to mount the adapter in a desired position relative to the front wall of the injector. An adapter includes a first section and a second section that are rotatable relative to each other about a hinge axis generally perpendicular to a longitudinal axis of the adapter. An adapter includes a first section and a second section that are generally the same in construction, the first section and the section being connectable to form a syringe carrier to seat at least a portion of the syringe.

CROSS-REFERENCE TO RELATED APPLICATION

[0001] This application is a continuation of application Ser. No.09/365,285, filed on Jul. 30, 1999, the contents of which are herebyincorporated by reference.

BACKGROUND OF THE INVENTION

[0002] The present invention relates to powered injector systems andsyringe adapters for use therewith.

[0003] A number of injector-actuated syringes and powered injectors foruse in medical procedures such as angiography, computed tomography,ultrasound and NMR/MRI have been developed. U.S. Pat. No. 4,006,736, forexample, discloses an injector and syringe for injecting fluid into thevascular system of a human being or an animal. Typically, such injectorscomprise drive members such as pistons that connect to a syringeplunger. For example, U.S. Pat. No. 4,677,980, the disclosure of whichis incorporated herein by reference, discloses an angiographic injectorand syringe wherein the drive member of the injector can be connectedto, or disconnected from, the syringe plunger at any point along thetravel path of the plunger via a releasable mechanism. A front-loadingsyringe and injector system is also disclosed in U.S. Pat. No.5,383,858, the disclosure of which is incorporated herein by reference.

[0004] As discussed in U.S. Pat. No. 5,383,858, a syringe used with afront-loading injector preferably includes a readily releasable mountingmechanism for securing the syringe to the front wall of the injector.The use of specifically designed mounting mechanisms, however, preventsthe use of syringes of other various types with front-loading injectors.Such syringes may, for example, include a syringe body, a plungerreciprocally mounted therein, and a plunger extension for transfer offorce to the plunger.

[0005] U.S. Pat. No. 5,520,653, the disclosure of which is incorporatedherein by reference, discloses several adapters designed to allow theuse of various syringes with a front-loading injector. In oneembodiment, the adapter of U.S. Pat. No. 5,520,653 includes a syringecarrier having a front end, a rear end, and syringe retaining channellocated between the carrier front and rear ends for engaging at least aportion of the syringe flange. Mounting flanges near the rearward end ofthe carrier releasably mount the carrier in a desired position relativeto the front wall of the injector. The adapter of U.S. Pat. No.5,520,653 further includes a follower reciprocally mounted within thecarrier. The follower has a front end that engages the syringe plungerextension when the syringe is installed in the carrier. A drive headopening in the carrier communicates with a pair of drive head slotspositioned near the rear end of the follower for releasably mounting thefollower in a desired position relative to the drive head of theinjector.

[0006] Although U.S. Pat. No. 5,520,653 is a substantial improvement inthe art, it remains desirable to develop improved adapters for use withsyringes of various types to permit use of such syringes withfront-loading injectors.

SUMMARY OF THE INVENTION

[0007] In general, the present invention provides an adapter forreleasably mounting a syringe in a desired position relative to afront-loading powered injector. The syringe includes a body and aplunger slideably positioned within the body. The injector includes afront wall, an opening formed in the front wall, and a drive memberreciprocally mounted in the injector. The adapter preferably includesgenerally a syringe carrier adapted to seat at least a portion of thesyringe. The syringe carrier includes at least one rearward facingabutment member to abut at least one forward facing surface on thesyringe. The syringe carrier includes an opening therein to allow thedrive member of the injector to communicate forward force to the plungerthrough abutment without connective engagement between the drive memberand the plunger. The adapter further includes a releasable mountingmechanism positioned to the rear of the syringe carrier to mount theadapter in a desired position relative to the front wall of theinjector.

[0008] The syringe may further include a transition region over whichthe radius or width of the syringe decreases (for example, a generallyfrusto-conical region) attached to a forward end of the body. Theabutment member may abut a forward facing surface created by thetransition region. Preferably, the abutment member abuts the transitionregion only in the vicinity of the transition from the body to thegenerally frusto-conical region (for example, at to the outer edge ofthe transition region).

[0009] The syringe may further include a syringe flange attached to arearward end of the body of the syringe. The abutment member may abut aforward facing surface of the syringe flange. Preferably, the abutmentmember abuts the syringe flange only in the vicinity of the transitionfrom the body to the syringe flange.

[0010] In one embodiment, the adapter includes a first section and asecond section rotatable relative to each other about a hinge axisgenerally perpendicular to a longitudinal axis of the adapter. The firstsection and the second section are preferably rotatable about the hingeaxis to an open position to allow loading of the syringe into theadapter from a position to the rear of the hinge axis. The first sectionand the second section are also preferably rotatable about the hingeaxis to a closed position to form the syringe carrier.

[0011] In another embodiment, the adapter includes a first section and asecond section that are generally the same in construction. The firstsection and the second section are connectable to form the syringecarrier and the releasable mounting mechanism.

[0012] The present invention also provides an adapter for releasablymounting a syringe in a desired position relative to a powered injector.The syringe preferably includes a body and a plunger slideably positionwithin the body as discussed above. The injector preferably includes afront wall, an opening formed in the front wall, and a drive memberreciprocally mounted in the injector. The adapter includes a firstsection and a second section that are rotatable relative to each otherabout a hinge axis generally perpendicular to a longitudinal axis of theadapter to an open position to allow loading of the syringe into theadapter from a position to the rear of the hinge axis. The first sectionand the second section are also preferably rotatable about the hingeaxis to a closed position to form a syringe carrier to seat at least aportion of the syringe.

[0013] The present invention also provides an adapter for releasablymounting a syringe in a desired position relative to a powered injector.The adapter preferably includes a first section and a second sectionthat are of generally the same in construction. The first section andthe section are connectable to form a syringe carrier to seat at least aportion of the syringe. Preferably, the first section and the sectionalso form a releasable mounting mechanism positioned to the rear of thesyringe carrier to mount the adapter in a desired position relative tothe front wall of the injector.

BRIEF DESCRIPTION OF THE DRAWINGS

[0014] Other aspects of the invention and their advantages will bediscerned from the following detailed description when read inconnection with the accompanying drawings, in which:

[0015]FIG. 1A illustrates an embodiment of an injector system of thepresent invention for use in connection with an MRI procedure.

[0016]FIG. 1B illustrates the injector system of FIG. 1A in which thesaline syringe and the adapter have been disassembled from the injector.

[0017]FIG. 2A illustrates a perspective view of an embodiment of anadapter of the present invention in an open state for loading of asyringe therein.

[0018]FIG. 2B illustrates a perspective view of the adapter of FIG. 2Ain an open state with a syringe loaded therein.

[0019]FIG. 2C illustrates a perspective view of the adapter of FIG. 2Ain a closed state with a syringe loaded therein.

[0020]FIG. 2D illustrates a plan view of the adapter of FIG. 2A in aclosed state with a syringe loaded therein.

[0021]FIG. 2E illustrates a side, cross-sectional view of the adapter ofFIG. 2A in a closed state with a syringe loaded therein.

[0022]FIG. 3A illustrates a perspective view of another embodiment of anadapter of the present invention in an open state for loading of asyringe therein.

[0023]FIG. 3B illustrates a perspective view of the adapter of FIG. 3Ain an open state with a syringe loaded therein.

[0024]FIG. 3C illustrates a perspective view of the adapter of FIG. 3Ain a closed state with a syringe loaded therein.

[0025]FIG. 3D illustrates a plan view of the adapter of FIG. 3A in aclosed state with a syringe loaded therein.

[0026]FIG. 3E illustrates a side, cross-sectional view of the adapter ofFIG. 3A in a closed state with a syringe loaded therein.

[0027]FIG. 4A illustrates a perspective view of another embodiment of anadapter of the present invention with a syringe positioned to beinserted therein.

[0028]FIG. 4B illustrates a perspective view of the adapter of FIG. 4Awith the syringe positioned therein.

[0029]FIG. 4C illustrates a perspective view of the adapter of FIG. 4Awherein a syringe retaining member is in a closed position.

[0030]FIG. 4D illustrates a perspective view of an adapter includinganother embodiment of a syringe retaining member.

[0031]FIG. 4E illustrates a perspective view of an adapter includinganother embodiment of a syringe retaining member.

[0032]FIG. 4F illustrates a perspective view of an adapter includinganother embodiment of a syringe retaining member.

[0033]FIG. 4G illustrates a perspective view of an adapter includinganother embodiment of a syringe retaining member.

[0034]FIG. 4H illustrates a perspective view of an adapter includinganother embodiment of a syringe retaining member.

[0035]FIG. 4I illustrates a perspective view of an adapter includinganother embodiment of a syringe retaining member.

[0036]FIG. 5A illustrates a perspective view of an embodiment of anadapter including separate, generally identical sections in anunconnected state.

[0037]FIG. 5B illustrates a perspective view of the adapter of FIG. 5Ain a connected state.

[0038]FIG. 6A illustrates a perspective view of another embodiment of anadapter including generally identical sections that are hinginglyattached via a side wall thereof.

[0039]FIG. 6B illustrates a front view of the adapter of FIG. 6A in anopen state.

[0040]FIG. 6C illustrates a perspective view of the adapter of FIG. 6Ain a closed state.

[0041]FIG. 7A illustrates a perspective view of another embodiment of anadapter including generally identical sections that are attached at afront end thereof in an open state.

[0042]FIG. 7B illustrates the adapter of FIG. 7A with a syringe loadedtherein.

[0043]FIG. 7C illustrates the adapter of FIG. 7A wherein the sectionsthereof have been hingingly closed for connection of the adapter to aninjector.

[0044]FIG. 8A illustrates a perspective view of a portion of an injectorhaving at least one removable face plate for attachment of a syringe oran adapter thereto.

[0045]FIG. 8B illustrates a perspective view of an embodiment of anadapter for use with the injector of FIG. 8A.

[0046]FIG. 8C illustrates a perspective view of another embodiment of anadapter for use with the injector of FIG. 8A.

[0047]FIG. 8D illustrates a perspective view of another embodiment of anadapter for use with the injector of FIG. 8A.

[0048]FIG. 8E illustrates a perspective view of another embodiment of anadapter for use with the injector of FIG. 8A.

[0049]FIG. 9A illustrates a perspective view of an embodiment of anadapter assembly or system in which a push rod performs the function ofa syringe plunger extension rod.

[0050]FIG. 9B illustrates a perspective view of the adapter assembly ofFIG. 9A in a disconnected state.

[0051]FIG. 9C illustrates a cross-sectional view of the adapter assemblyof FIG. 9A.

DETAILED DESCRIPTION OF THE INVENTION

[0052] An embodiment of a front-loading injector system 5 of the presentinvention is illustrated in FIGS. 1A and 1B. Injector system 5 isparticularly adapted for use in MRI procedures and includes a poweredinjector 10, a syringe 20 for injection of saline solution and anadapter 100. An example of an injector 10 suitable for use in thepresent invention is the SPECTRIS® injector available from Medrad, Inc.of Indianola, Pa. However, the present invention may be used inconnection with other fluid delivery systems, including injectors andinfusion pumps for computed tomography, ultrasound and angiographicprocedures. As best illustrated in FIG. 1B, injector housing 30 ofinjector 10 preferably includes a first drive member or piston 40therein which cooperates with a syringe plunger 50 in saline syringe 20to inject a saline solution from the interior of syringe 20 into apatient.

[0053] As shown in FIG. 1B, injector 10 also includes a second drivemember or piston 40′ that cooperates with an adapter 100 and a syringeplunger extension rod 220 of a syringe 200 (see, for example, FIG. 2A)containing a fluid such as a contrast medium to inject the fluid fromthe interior of syringe 200 into a patient.

[0054] As used herein to describe injection system 5 and otherembodiments of the present invention, the terms “axial” or “axially”refer generally to, for example, an axis A around which adapter 100 ispreferably formed (although not necessarily symmetrically therearound)or an axis B around which saline syringe 20 is formed (although notnecessarily symmetrically therearound). The terms “proximal” or“rearward” refer generally to an axial or a longitudinal directiontoward the end of injector housing 30 opposite the end to which syringe20 and adapter 100 are mounted. The terms “distal” or “forward” refergenerally to an axial or a longitudinal direction toward a syringe tipof syringe 20 or syringe 200. The term “radial” refers generally to adirection normal to an axis such as axis A or axis B.

[0055] Saline syringe 20 and adapter 100 are preferably removablyconnected to injector 10 as described in U.S. Pat. No. 5,383,858. Inthat regard, front-loading injector 10 preferably includes a front wall60 having a first opening 62 formed therein. Piston 40 is reciprocallymounted within injector 10 and is extendible through opening 62. Piston40 preferably includes a piston flange or head 44. Receiving slots 66 aand 66 b, are preferably positioned opposite one another around opening62. Receiving flanges 68 a and 68 b are preferably positioned oppositeone another and between receiving slots 66 a and 66 b and extendinwardly into opening 62.

[0056] The rearward end of saline syringe 20 preferably includes areadily releasable mounting mechanism such as a pair of mounting flanges22 a and 22 b for mounting saline syringe 20 in a desired positionrelative to the front wall 60 of injector 10. Flange 22 b is not shownbut is generally identical to flange 22 a and positioned opposite flange22 a. Mounting flanges 22 a and 22 b may include indicating means, suchas detent(s), bar code(s), protrusion(s) or notch(es) 24 a, whichprovide information to the injector 10, for example, about the type ofsaline syringe 20 being used. Correspondingly, injector 10 preferablyincludes any suitable means (not shown) for reading information fromnotch(es) 24 a.

[0057] To attach syringe 20 to injector 10, the rearward end of syringe20 is inserted into injector opening 62 such that mounting flanges 22 aand 22 b are inserted into receiving slots 66 a and 66 b, respectively.If, at this time, plunger 40 is not positioned at the rearward end ofsyringe 20 such that a piston flange 44 can engage capture members 54(as described in U.S. Pat. No. 5,383,858), piston 40 may be advancedforward by the operation of injector 10 until piston flange 44 is inposition to be received by capture members 54.

[0058] Once mounting flanges 22 a and 22 b are inserted into receivingslots 66 a and 66 b, respectively, and piston 40 is in position to bereceived by capture members 54, the operator preferably rotates syringe20 approximately 90 degrees such that mounting flanges 22 a and 22 bmove behind and are engaged by receiving flanges 68 a and 68 b,respectively, and piston flange 44 rotates into position to be retainedby, for example, L-shaped capture members 54. Injector 10 may include astop mechanism (not shown), for example, extending from at least one ofthe retaining slots 68 a and 68 b, to prevent rotation of syringe 20more than 90 degrees. Tactile, visual or audible feedback can beprovided to the operator via, for example, cooperating members onsyringe 20 and injector 10 to inform the operator that secure connectionhas been achieved. After securely attaching syringe 20 to injector 10,advancing piston 40 in a forward direction will apply a motive force toplunger 50 to advance plunger 50 forward within syringe 20, therebyforcing saline solution in syringe 20 out of syringe neck 26 into thefluid path to the patient. Retracting piston 40 in a rearward directionwill cause plunger 50 to move rearward in syringe 20, thereby drawingfluid into syringe 20.

[0059] Adapter 100 is preferably attached to injector 10 in a similarmanner as described above for attachment of syringe 20 to injector 10.In that regard, a rearward portion or section of adapter 100 preferablyincludes a readily releasable mounting mechanism such as a pair ofmounting flanges 102 a and 102 b (see FIG. 2A) for mounting adapter 100in a desired position relative to the front wall 60 of injector 10.Mounting flanges 102 a and 102 b may include indicating means, such asdetents or notches 104 a and 104 b, which provide information toinjector 10 about the type of adapter and/or syringe being used.Correspondingly, injector 10 preferably includes any suitable means (notshown) for reading information from notches 104 a and 104 b.

[0060] To attach adapter 100 to injector 10, the rearward end of adapter100 is inserted into injector opening 62′ such that mounting flanges 102a and 102 b are inserted into receiving slots 66 a′ and 66 b′,respectively. Once mounting flanges 102 a and 102 b are inserted intoreceiving slots 66 a′ and 66 b′, respectively, the operator preferablyrotates adapter 100 or adapter 100/syringe 200 combination approximately90 degrees such that mounting flanges 102 a and 102 b move behind andare engaged by receiving flanges 68 a′ and 68 b′, respectively. Asdescribed above, a stop mechanism (not shown) may, for example, extendfrom at least one of the retaining slots 68 a′ and 68 b′, to preventrotation of adapter 100 more than 90 degrees. Once again, tactile,visual or audible feedback can be provided to the operator via, forexample, cooperating members on adapter 100 and injector 10 to informthe operator that secure connection has been achieved. A drip flange 106can, for example, be formed on a rearward portion of adapter 100 to,among other things, assist in forming a secure connection. Drip flange106 may, for example, include a raised member or detent 108 (see, forexample, FIG. 2A) that mates with a recess (not shown) in the face ofopening 62′ to provide audible and/or tactile feedback to the operatorupon proper alignment/connection of adapter 100 to injector 10.

[0061] After securely attaching adapter 100 to injector 10, advancingpiston 40′ in a forward direction will apply a motive force to a plungerextension 220 of syringe 200 to a advance syringe plunger 225 (see FIG.2E) forward within syringe barrel 210, thereby forcing contrast mediumin syringe 200 out of syringe neck 250 into the fluid path to thepatient.

[0062] Adapter 100 is illustrated in further detail in FIGS. 2A through2E. In the embodiment of adapter 100, a “break” action is used to loadsyringe 200 into a carrier 110 of adapter 100. In that regard, carrier110 includes a first portion or section 120 and a second portion orsection 130. First portion 120 is hingingly attached to second portion130 via support arms 132 a and 132 b, each of which includes a passage134 therein. First portion 120 includes generally cylindrical tabs 122on each side thereof that snap into passages 134 to hingingly orrotatably attach first portion 120 to second portion 130 about an axis C(see, for example, FIG. 2D) preferably oriented generally perpendicularto longitudinal axis A of adapter 100.

[0063]FIG. 2A illustrates adapter 100 in an open state and ready toreceive syringe 200 from a position to the rear of the hingingmechanism. In this embodiment, syringe 200 comprises generallycylindrical body or barrel 210 in which a fluid such as contrast medium,saline or therapeutic agent is contained. Preferably, the fluid mediumis “prefilled” into syringe 200 before loading of syringe 200 in adapter100. Syringe 200 can, for example, be prefilled by the manufacturer ormanually filled remote from the injector. Syringe 200 further includesplunger 225 slideably disposed within barrel 210 that is similar inoperation to plunger 50 of saline syringe 20. Plunger 225 of syringe 200is operatively connected to plunger extension rod 220 by, for example, athreaded connection. Syringe 200 further includes a flange 230 at arearward end of barrel 210. At a forward end of barrel 210, syringe 200includes a generally frusto-conical transition or cone region 240 thatconnects barrel 210 to a tapered neck 250 from which contrast medium isinjected. Tapered neck 250 can include, for example, a luer connectionat the end thereof for connection to a fluid path (for example, flexibletubing) as known in the art.

[0064] In many cases, syringes 200 for use, for example, in an MRIprocedure are prefilled with contrast medium by the manufacturer. Manysuch syringes 200 are designed for manual injection into a patientwherein an operator manually advances plunger rod 220 (and therebyplunger 225 within syringe 200) forward by applying pressure to arearward end 228 of plunger extension rod 220. Syringe barrel 210 andflange 230 may, for example, be fabricated from glass or plastic.Plunger extension rod 220 is typically fabricated from a plasticmaterial.

[0065] As illustrated in FIGS. 2A and 2B, syringe 200 is loaded intocarrier 110 by positioning syringe 200 in general alignment with agenerally cylindrical passage 140 formed in a forward end of firstportion 120 of adapter 100. Syringe 200 is slid forward within passage140 until syringe flange 230 abuts a shoulder 150 (see FIG. 2E) thatextends radially inwardly within first portion 120. Shoulder 150cooperates with syringe flange 230 to hold syringe 200 within adapter100 and to provide resistance to the forward force applied to plungerextension rod 220 by piston 40′ during an injection procedure.

[0066] As best illustrated in FIG. 2E, shoulder 150 preferably includesa rearward extending ridge portion 154 on the inner radius thereof sothat ridge portion 154 contacts flange 230 only near or in the vicinityof the transition of syringe flange 230 into syringe barrel 210. Contactof ridge portion 154 with syringe flange 230 near barrel 210 assists inminimizing the forces placed upon cantilevered flange 230. For example,in the case of glass syringes 200, flange 230 may fail (break) ifcontact with shoulder 150 is made at or near the outer end of syringeflange 230, whereas the shorter lever arm resulting from contact withsyringe flange 230 at or near the inner radius thereof will reduce theforce on syringe flange 230 and prevent failure. Ridge portion 154 canbe made of a resilient or compliant material such as an elastomericmaterial that can be different from the material of the remainder ofadapter 100 to further reduce the likelihood of failure.

[0067] In the case of a prefilled syringe 200, there is no need for theoperator to retract the plunger of syringe 200 to load syringe 200 withcontrast medium. Therefore, there is usually no need for a followermechanism in the adapter of the present invention to attach to plungerextension rod 220 to enable retraction of plunger 225 as described inconnection with the adapter of U.S. Pat. No. 5,520,653. Piston 40′ cansimply be advanced to abut rearward surface 228 of plunger extension rod220. Any further forward motion of piston 40′ will result in advancementof the plunger of syringe 200 and pressurization of the contrast mediumwith syringe 200. Elimination of a carrier mechanism for the plungerextension simplifies and reduces the cost of manufacture of the adaptersof the present invention as compared, for example, to the adapter ofU.S. Pat. No. 5,520,653. Nevertheless, the adapters of the presentinvention may readily be configured with follower mechanisms thatconnect to plunger extension rods 220 to allow plunger retraction.

[0068]FIGS. 2C through 2E illustrate syringe 200 within adapter 100 withfirst portion 120 and second portion 130 in a closed position. Adapter100 preferably includes a mechanism to assist in maintaining firstportion 120 and second portion 130 in a closed position during operationof injector 100. Second portion 130 may, for example, include a latchtab 136 having an abutment shoulder 138 that cooperates with a recess128 in a rearward end of first portion 120 to create a snap latchingmechanism. Many other closing mechanisms can be used to maintain firstportion 120 and second portion 130 in a closed position, as clear to oneskilled in the art.

[0069] Closed carrier 110 created by first portion 120 and secondportion 130 also functions to limit the motion of plunger extension rod220 out of alignment with axis A. This prevents plunger extension rod220 from, for example, slipping out of contact with piston 40′, preventsdeforming of plunger extension rod 220 and prevents eccentric loading ofplunger extension rod 220. Deflection, eccentric loading or deforming ofplunger extension rod 220 may, for example, cause leaking of fluid tothe rear of plunger 225 or breaking of syringe 200. Radially inwardprojecting guide(s) can be formed in one or both of first portion 120and second portion 130 to maintain even tighter tolerances. A section ofeither or both of first portion 120 and second portion 130 can be “cutaway” to form a window for viewing of syringe extension rod 220.Likewise, a portion or the entirety of either or both first portion 120and second portion 130 can be transparent.

[0070] Preferably, one or both of first portion 120 and second portion130 includes an abutment member to prevent rotation of syringe 200within carrier 110. It is, for example, desirable to prevent rotation ofsyringe 200 after connection thereof to fluid path tubing. Prevention ofsyringe rotation can also maintain syringe 200 in proper orientation forviewing, for example, volume gradations on syringe 200. One or moresides of first portion 120 can, for example, have a flattened profile toconform to flattened section(s) 234 of syringe flange 230 to preventrotation of syringe 200.

[0071] As illustrated in FIGS. 2B through 2E, a substantial portion ofsyringe 200 extends forward through passage 140 so that syringe barrel210 is plainly visible to the operator. Such visibility, for example,facilitates reading of wording printed on the syringe as well as visualdetermination of the volume of contrast remaining in syringe 200.Visibility of syringe 220 also allows the operator to more readilydetermine whether air is present in syringe 200 before commencing aninjection procedure. Moreover, operators typically like to see plunger225 in motion to provide reassurance that the injection is proceeding.Extension of a portion of syringe 200 beyond carrier 110 alsofacilitates grasping of syringe 200 by the operator to, for example,connect or disconnect a fluid path to syringe neck 250.

[0072] As illustrated, for example, in FIGS. 2A through 2C, axis C ofrotation of the hinge mechanism (that is, the axis passing through theradial center of generally cylindrical tabs 122 in the embodiment ofFIG. 2A) is preferably positioned such that the force experienced bycarrier 110 during forward advancement of piston 40′ tends to force ormaintain carrier 100 in a closed position. The axis of cylindrical tabs122 is preferably, for example, positioned above the center line orlongitudinal axis of carrier 110 such that a forward force exerted onshoulder 150 tends to produce a torque that maintains first portion 120in a latched, closed position relative to second portion 130.

[0073] Once an injection procedure is completed, the operator can graspthe adapter or adapter/syringe combination and rotate it 90 degrees backto the pre-installation orientation, thereby, disengaging mountingflanges 102 a and 102 b from behind receiving flanges 68 a and 68 b,respectively. The adapter/syringe combination is then removable from theinjector 10.

[0074] Retaining syringe 200 within carrier 110 by abutment withshoulder 150, allows accommodation of many different designs of syringe200 by carrier 110. Adapter 100 is thus usable with a wide variety ofcurrently available syringes 200.

[0075]FIGS. 3A through 3E illustrate another embodiment of an adapter300 for use with a syringe 200. The rearward portion of adapter 300 isessentially identical to that of adapter 100 and is removably attachedto injector 10 as described above. Unlike adapter 100, which holdssyringe 200 within adapter 100 and provides resistance to the forwardforce applied to plunger extension rod 220 by abutment of syringe flange230, syringe 200 is held within adapter 300 and resistance provided tothe forward force applied to plunger extension rod 220 by abutting aforward facing surface of forward transition region 240 of syringe 200rather than by abutting or retaining syringe flange 230.

[0076] Like adapter 200, a hinging or “break” action is used to loadsyringe 200 into a carrier 310 of adapter 300. In that regard, carrier310 includes a first portion 320 and a second portion 330. First portion320 is hingingly or rotatably attached to second portion 330 via supportarms 332 a and 332 b, each of which includes a passage 334 therein.First portion 320 includes generally cylindrical tabs 322 on each sidethereof that reside in passages 334 to hingingly attach first portion320 to second portion 330. First portion 320 rotates about an axis Cthat runs generally through the radial centers of tabs 322 and isgenerally perpendicular to the longitudinal axis A of adapter 300.

[0077]FIG. 3A illustrates adapter 300 in an open state and ready toreceive syringe 200. As illustrated in FIGS. 3A and 3B, syringe 200 isloaded into carrier 310 by positioning syringe 200 in general alignmentwith a generally cylindrical passage 340 formed in first portion 320 ofadapter 300. Syringe 200 is slid forward within passage 340 until aforward facing surface of syringe 200 abuts a retention shoulder 350(see FIG. 3E) that extends radially inward at a forward end of a forwardportion 342 of first portion 310. Shoulder 350 cooperates with forwardsyringe transition region or cone 240 to hold syringe 200 within adapter300 and to provide resistance to the forward force applied to plungerextension rod 220 by piston 40′ during an injection procedure. Asillustrated in detail D of FIG. 3E, shoulder 350 preferably contactssyringe 200 only near to or in the vicinity of the transition from thesidewall of barrel 110 to transition region 240 to take advantage ofincreased structural strength in this region. The contact area ofshoulder 350 can be made of a resilient or compliant material (forexample, an elastomeric material) to absorb energy and reduce thelikelihood of breaking syringe 200.

[0078] Syringe 200 may be inserted in adapter 300 before connection ofadapter 300 to injector 10. Alternatively, syringe 200 may be loadedinto adapter 300 while adapter 300 is mounted on injector 10. Indeed,adapter 300 may remain mounted on injector 10 through many differentinjection procedures with different syringes.

[0079] Forward portion 342 preferably includes one or more open areas orwindows 344 so that syringe barrel 210 is plainly visible to theoperator. All or a portion of forward portion 342 can also betransparent to further facilitate viewing of syringe barrel 210. Openareas 344 also facilitate grasping of syringe 200 by the operator to,for example, connect or disconnect a fluid path to syringe neck 250. Asdescribed in connection with adapter 100, one or both of first portion320 and second portion 330 may include an abutment member to preventrotation of syringe 200 within carrier 310. For example, the side(s) offirst portion 320 can have a flattened profile to conform to flattenedsection(s) 234 of syringe flange 230 to prevent rotation of syringe 200.The cooperation of such a flattened profile of carrier 310 and section234 can, for example, be used to ensure a desired orientation of syringebarrel 210 with open areas 344. For example, two open areas 344 can beprovided generally opposing each other (that is, positionedapproximately 180° apart on forward portion 342). The cooperation of aflattened profile of carrier 310 and flattened syringe flange section234 in this embodiment preferably allows mounting of syringe 200 incarrier 310 in only two axially rotated orientations, 180° apart.

[0080] One or a plurality of inward projecting guide 360 can be formedin one or both of first portion 120 and second portion 130 to maintain atight tolerances to prevent deflection of plunger extension rod 330 asdiscussed above. A plurality (for example, three) guides 360 can be usedabout first portion 120 and/or second portion 130 to limit or preventdeflection in any direction.

[0081] Open areas (not shown) can also be provided on carrier 310 in thearea where syringe flange 230 resides to accommodate large (in a radialdirection) or irregularly shaped syringe flanges 230. Such open areaspreferably extend longitudinally to accommodate syringes of differentlength from a forward end thereof to the syringe flange thereof. Ingeneral, the adapters of the present invention preferably provideadequate capacity to accommodate syringes of widely varying length,diameter, etc.

[0082] An important function of an injector is to monitor and report theactual volume of fluid available for delivery within a syringe. Thisfunction, for example, enables rapid decision on whether enough fluid ispresent to proceed with an imaging procedure or whether additionalvolume should be loaded. Monitoring the cumulative volume of fluiddelivered to a patient is also desirable for certain applications wherea recommended per-patient dosage volume should not be exceeded. Fluidvolumes delivered by injectors are typically displayed in 1.0 mlincrements and are tracked by the injector with finer resolution than isdisplayed. Injectors also preferably detect and differentiate amongdifferent types and sizes of syringes so that accurate display anddelivery of fluid volume is provided.

[0083] To achieve such fluid volume management specifications, anadapter or syringe must be installed on an injector, be oriented in aknown manner and provide the control system with identificationinformation. Identification can be provided by coded features on theadapter or syringe that are detected by sensors on the injector so thateach adapter and/or syringe is known by its code and fluid volumeparameters specific to that syringe are implemented. When syringes 200that are intended for non-powered, hand injection are installed on powerinjector 10, adequate identification is still preferably provided. Thisresult can be achieved by first placing syringe 200 in adapter 100 or300 which facilitates mounting on injector 10 and possesses its ownunique code as encoded by, for example, the positions of notches 104 aand 104 b. In this manner, many different types and sizes of syringes200 and/or adapters can be accommodated.

[0084] Syringes 200 are frequently of similar geometry such that morethan one type of syringe 200 can be carried by the same adapter, givingrise to the potential of incorrect identification and possible fluiddelivery error by injector 10. However, it is desirable to minimize thenumber of adapters required to accommodate all the hand syringesintended for a specific injector leading to a need to install more thanone volume of syringe per adapter, provided individual functionality canbe achieved. Syringes that share the same functional internal diameter,but have different lengths of travel can be treated as equivalent ifboth are referenced to the adapter, and consequently to injector 10, bya front-most surface thereof (that is, cone or transition region 240).If syringes 200 sharing the same functional diameter but havingdifferent lengths are referenced to the adapter injector 10 by rearflange 230 only, injector 10 will not be able to determine where thefront of a syringe 200 is and cannot accurately determine/report thevolume of contrast medium available. Mounting hand syringes 200 by rearflange 230 as in the embodiment of adapter 100 thus preferably requiresone adapter per syringe diameter and length combination, which resultsin a larger number of adapters than would be required using a frontmounting as in the embodiment of adapter 300. Multiple adaptercombinations decrease the ease of use for an operator and expand thelogic and sensing capacity required of injector 10. An optimum approachwould be to use a single adapter that accommodates all hand syringestargeted for a particular injector. To approach this goal, it ispreferable to retain/abut a front end of syringes 200 as described abovein connection with adapter 300 so that injector 10 can determine theposition of the front end of syringe 200. Loading of a front end ofsyringe 200 is also preferred to take advantage of an area of increasedsyringe strength to prevent syringe failure.

[0085]FIGS. 4A through 4C illustrate another embodiment of an adapter400 for use with syringe 200. The rearward portion of adapter 400 isessentially identical to that of adapters 100 and 300 and is removablyattached to injector 10 as described above. Unlike adapters 100 and 300,which incorporate a hinging action to enclose syringe 200, syringe 400includes an open carrier 410. Like adapter 300, however, syringe 200 isheld within adapter 400 and resistance provided to the forward forceapplied to plunger extension rod 220 by abutting forward transition orcone region 240 of syringe 200.

[0086] As illustrated in FIGS. 4A and 4B, syringe 200 is simply loadedinto adapter 400 by dropping syringe 200 therein from above. Adapter 400preferably includes a first, rearward portion 420 that seats/supportssyringe flange 230. Preferably, first portion 420 has generally flatside walls 422 that cooperate with generally flat sections 234 onsyringe flange 230 to restrict or substantially prevent rotation ofsyringe 200 within adapter 400. Side walls 422 of first portion 420preferably extend upward past the generally common axis of syringe 200and adapter 400 to assist in supporting syringe 200.

[0087] Adapter 400 further includes a second, forward portion 430 thatseats/supports syringe barrel 210. Second portion 430 preferablyincludes a radially inward extending abutment shoulder 450 that abutscone or transition region 340 of syringe 200 to retain syringe 200within adapter 400 and provide resistance to the forward force appliedto plunger extension rod 220 by piston 40′. Although second portion 430,including abutment shoulder 450, are open on the top thereof, thegenerally cylindrical wall of second portion 430 and abutment shoulder450 preferably extend upward past the generally common axis of syringe200 and adapter 400 to support resistance of the forward force appliedto plunger extension rod 220 and to prevent deflection of syringe 200out of alignment with the shared axis of syringe 200 and adapter 400.

[0088] Through abutment shoulder 450, adapter 400 provides the benefitsof forward abutment of syringe 200 discussed above. Moreover, becauseadapter 400 is open along its entire axial length, insertion and removalof syringe 200 is facilitated. For example, syringe 200 can even beeasily removed from adapter 400 while still connected to a fluid path(not shown in FIGS. 4A through 4C). In some cases, however, it may bedesirable to form abutment shoulder 450 to contact a forward facingsurface of transition region 240 around its entire circumference toprovide additional stability. In that case, the forwardmost end ofcarrier 410 would be closed and any fluid path would preferably bedisconnected before removing syringe 200 from adapter carrier 410.

[0089] Adapter 400 preferably further includes at least one retainingmember 460 to assist in retaining and/or stabilizing syringe 200 inproper alignment therein. Retaining member 460 is slideably retained ina generally cylindrically shaped passage 470 in carrier 410. Retainingmember 460 is illustrated in an open or disengaged position in FIGS. 4Aand 4B. To close or engage retaining member 450 to retain syringe 200,the operator can supply force to collar tab 462 to rotate retainingmember 450 within passage 470 to a closed position as illustrated inFIG. 4C. In another embodiment illustrated in FIG. 4D, rotatableretaining member 460 can be split into two portions 460′ and 460″ thatrotate to meet in the middle.

[0090] Other retaining/stabilizing members or mechanisms forretaining/stabilizing syringe 200 are illustrated in FIGS. 4E through4I. In FIG. 4E a sliding retaining member 460 a is positioned on/aroundsecond, forward portion 430 of carrier 410. Retaining member 460 a ispreferably positioned at a forwardmost position on second portion 430when syringe is loaded into carrier 410 to facilitate loading. Retainingmember 460 a is retained on second portion 430 by abutment with aforward shoulder 480 and rearward shoulder 482. After seating of syringe200, retaining member 450 a can preferably be slid to any desiredposition on second portion. Positioning retaining member 460A at arearwardmost position on second portion 430 may maximize stability.Retaining member 460 a preferably conforms closely to the shape ofsyringe barrel 210 to maximize stability. Retaining member 460 a mayinclude an open section 462 a on the top thereof to facilitate removalof syringe 200 from carrier 410 without disconnection of an attachedfluid path element.

[0091]FIG. 4F illustrates another embodiment of a slideable retainingmember 460 b. Retaining member 460 b is slideably retained upon firstportion 420 of carrier 410 between drip flange 106 and shoulder 484. Tofacilitate loading of syringe 200, retaining member 450 b may bepositioned near drip flange 106. After loading of syringe 200, retainingmember 460 b can be slid to a desired position. An opening (not shown)in retaining member 460 b can be formed to facilitate removal of syringe200 from carrier 410 without disconnection of an attached fluid pathelement.

[0092] In the embodiment of FIG. 4G, a retaining mechanism includes twocantilevered retaining member 460 c′ and 460 c″ that snap around syringebarrel 210 upon loading of syringe 200 in carrier 410.

[0093] A plurality of retaining/stabilizing members as described abovecan be provided along the length of carrier 410 to assist inretaining/stabilizing syringe barrel 210 and plunger extension rod 420in proper position within carrier 410. The opening and closing of suchretaining members can be operated individually or collectively, forexample, via a common tab.

[0094] Alternatively, a retaining/stabilizing member can be increased inaxially length to increase stability. For example, FIG. 4H illustrates aretaining member 460 d hingingly attached to first portion 420 thatextends along the entire length of first portion 420 and partially alongthe length of second portion 430 when closed. A similar retaining membercan alternatively or additionally be hingingly attached to secondportion 430. As an alternative to a hinging motion, such retainingmember can rotate in a passage or slot formed in carrier 410.

[0095] An example of a widened, rotating retaining member 460 e isillustrated in FIG. 4I. Retaining member 460 e is rotatably attached(about the longitudinal axis of carrier 410) to second portion 430 andextends generally along the entire length of second portion 430. Aftersyringe 200 is top loaded into carrier 420, retaining member 460 e canbe rotated to form a cover over second section 430. Retaining members460 d and 460 e can be transparent or formed with cut away sections toenhance the visibility of syringe 200.

[0096] In some cases it may be desirable to manufacture the adapter ofthe present invention to be disposable after one or more uses. Suchdisposable adapters are preferably manufactured in an inexpensivemanner. In FIGS. 5A and 5B, an embodiment of a preferably disposableadapter 500 is illustrated. Adapter 500 preferably includes twogenerally identical members 510 a and 510 b. Fabricating adapter 500from two generally identical members 510 a and 510 b may substantiallyreduce manufacturing costs. Members 510 a and 510 b may for example befabricated to “snap” together (for example, via extension members 520and cooperating catch members 530) and provide visible, audible and/ortactile feedback to indicated proper connection.

[0097] In use, syringe 200 is preferably seated in one of members 510 aor 510 b. The other portion is then, for example, snapped into place toencompass syringe 200 within the resultant adapter 500 (see FIG. 5B).When assembled, portions 510 a and 510 b form a rearward section thathouses plunger extension rod 220 and a forward portion that housessyringe barrel 210. At or near a rearward end of adapter 500, members510 a and 510 b preferably form a connecting section including firstmounting flange 502 a and a second mounting flange 502 b adapted toremovably attach adapter 500 to injector 10 as described above. Asillustrated in FIG. 5b, adapter 500 encompasses both syringe barrel 210and plunger extension rod 220 to retain/stabilize syringe 200. The sidewalls of adapter 500 can be formed with a generally flat or flattenedprofile to interact with/abut generally flat section(s) 234 of syringeflange 230 to prevent rotation of syringe 200 about its axis withinadapter 200.

[0098] To facilitate viewing of either plunger extension rod 220 orbarrel 210, adapter 500 can be formed with cut out window sections 540.Moreover, any portion or all of adapter 500 can be transparent.

[0099] Adapter 500 provides resistance to the forward force applied toplunger extension rod 220 by abutment of syringe transition region 240with a radially inward extending shoulder section 550. The advantages ofproviding such resistance/retention by abutment of syringe transitionregion 240 discussed above in connection with other embodiments ofadapter of the present invention are also provided by adapter 500.

[0100] Another embodiment of an adapter 500′ is illustrated in FIGS. 6Athrough 6C. Adapter 500′ is generally identical to adapter 500 exceptthat adapter 500′ is formed from the connection of a first portion 510a′ and a second portion 510 b′ that are initially hinged together, forexample by a notched plastic hinge 512 as known in the art) as bestillustrated in FIGS. 6A and 6B.

[0101]FIGS. 7A through 7C illustrate another embodiment of an adapter600 of the present invention. Adapter 600 includes a first member 610 aand a second member 610 b that are attached via a forward hingemechanism. The hinge mechanism preferably includes a generallycylindrical member 612 on an extending member 614 of one of first member610 a and second 610 b that is rotatably seatable in a passage 616formed in an extending member of the other of first member 610 a andsecond member 610 b. Extending members 614 preferably extend forward oneach side of a forward end of each of first member 610 a and secondmember 610 b as illustrated in FIG. 7A.

[0102] First member 610 a includes first retaining flange 102 a asdescribed above, while second member 610 b includes second retainingflange 102 b that operate to connect adapter 600 to injector 10 asdescribed above. First member 610 a preferably includes one half of adrip flange 106 a, while second member 610 b preferably includes theother half of a drip flange 106 b.

[0103] To seat syringe 200 within adapter 600, first member 610 a andsecond member 610 b are preferably rotated about an axis C′ of hingingmechanism (which axis is generally perpendicular to the orientation oflongitudinal axis A′ of adapter 600) to an open position as illustratedin FIGS. 6A and 6B. Barrel 210 of syringe 200 is then passed through anopening 640 formed at the forward end of adapter 600. Syringe 200 isadvanced forward through passage 640 until flange 230 abuts radiallyinward extending shoulder 650 to retain syringe 200 within adapter 600and provide resistance to forward force exerted upon plunger extensionrod 220 by piston 40′. First member 610 a and second member 610 b arethen rotated to a closed position. As discussed above in connection withadapter 100, shoulder 650 may include a raised (rearward extending)abutment ridge 660 to ensure that contact is made with syringe flange230 near the point where syringe flange 230 is connected to barrel 210.Forward force exerted upon shoulder 650 assists in maintaining adapter600 in a closed position as illustrated in FIG. 6C.

[0104] Like adapters 500 and 500′, first member 610 a and second member610 b can be formed to be generally identical. Fabrications costs ofadapter 600 can thereby be reduced.

[0105] In all of the embodiment discussed above, the adapter is attachedto injector 10 via mounting flanges on a rearward portion or section ofthe adapter. There are, however, alternative manners in which an adapterof the present invention may be attached to injector 10. As illustratedin FIG. 8A, for example, an injector may include a front wall 700 towhich at least one removable face plate 705 is attached. The injector ofFIG. 8A is designed for use in an MRI procedure and includes a first,contrast syringe 710 attached to a first face plate 705 and a second,saline syringe 720 attached to a second face plate 705′. In theembodiment of FIG. 8A, face plate 705 is rotated upward to be detachedfrom the injector.

[0106]FIG. 8B illustrates an embodiment of an adapter 800 including acarrier 810 formed integrally or attached to a face plate 805 suitablefor attachment to the injector of FIG. 8A. Syringe 200 can be “breach”loaded into carrier 810 by first tilting syringe 200 and advancingbarrel 210 of syringe 200 in a forward direction through passage 840formed in a forward most position of an enclosed forward section 830 ofcarrier 810. Syringe 200 is advanced until syringe cone region 240 abutsradially inwardly extending shoulder 850 that defines passage 840. Faceplate 805 includes a passage 808 therein through which a piston (notshown) of the injector of FIG. 8A can pass to cooperate with plungerextension rod 220.

[0107]FIG. 8C illustrates an embodiment of an adapter 900 that includesa carrier 910 attached to a removable face plate 905. In thisembodiment, syringe 200 is advanced through passage 908 in face plate902. Syringe 200 is advanced forward until cone region 240 abutsradially inward extending shoulder 950 of carrier 910.

[0108]FIG. 8D illustrates an embodiment of an adapter 1000 that includesa carrier 1010 attached to a removable face plate 1005. Syringe 200 isloaded into carrier 1010 from the top by dropping syringe 200 intocarrier 1010. When seated in carrier 1010, syringe 200 abuts radiallyinward extending shoulder 1050 of carrier 1010. The top of carrier 1010is maintained in an open state over the length of carrier 1010 tofacilitate removal of syringe 200 even when connected to a fluid pathelement.

[0109]FIG. 8E illustrates an embodiment of an adapter 1100 that includesa carrier 1110 attached to a removable face plate 1105. Like adapter1010, syringe 200 is loaded into carrier 1110 from the top by droppingsyringe 200 into carrier 1110. When seated in carrier 1110, syringetransition region 240 abuts radially inward extending shoulder 1150 ofcarrier 1110. Carrier 1110 includes a hinging cover section 1160 thatcan be rotated to a closed position to form a cover/retainer over atleast a portion of syringe barrel 210 to assist in retaining/stabilizingsyringe 200. Shoulder 1050 can be rotatable to capture syringe 200 andsupport it.

[0110]FIGS. 9A through 9C illustrate an embodiment of an adapter system1200 including a carrier section 1210, an intermediate section 1220, anda rearwardmost connecting section 1230. Adapter 1200 further includes apush rod 1240. Syringe 200 is seated in carrier section 1210 by droppingsyringe 200 into carrier section 1210. Cone region 240 abuts shoulder1250 of carrier section 1210. The plunger extension rod (not shown) hasbeen removed from connection with syringe plunger 225. In many cases,such plunger extension rods are connected to plunger 225 via threadingon the forward end of the plunger extension rod.

[0111] Push rod 1240 extends through intermediate section 1220 tocooperate with plunger 225 to apply force to plunger 225. In the case ofa prefilled syringe, there is typically no need to retract plunger 225within syringe 200. In such cases, there is no need to establish anengaging connection (threaded or otherwise) between a forward end ofpush rod 1240 and plunger 225 to resist the force of and couple plunger225 to push rod 1240 during a retracting motion of push rod 1240. Thisgreatly simplifies the construction and operation of push rod 1240 andthe injector.

[0112] In operation of adapter system 1200, push rod 1240 makes aconnection with a piston (not shown in FIGS. 9A through 9C; see FIG. 1A)of the injector through a connective coupling 1242 on a rearward end ofpush rod 1240. Connecting section 1230 is removably attached to theinjector via the cooperation of mounting flanged 1202 a and 1202 b anddrip flange 1206 with the injector as described above. Syringe 200 canbe top loaded into carriage section 1210 either before or afterconnection of adapter 1205 to the injector via connecting section 1230.Push rod 1240 is advanced forward through intermediate section 1220 bythe injector piston until forward end 1244 pilots into syringe plunger225 to abut a rearward facing wall section within plunger 225. Onceagain, no secured connection to resist a rearward motion need beeffected between push rod forward end 1244 and plunger 225 in, forexample, the case of a prefilled syringe or in any other case thatretraction of plunger 225 within syringe 200 will not be required. Pushrod forward end 1244 is preferably of generally the shape of therearward facing interior of plunger 225. In this manner, push rodforward end 1244 provides support to plunger 225 to maintain the shapeof plunger 225 during use of syringe 200. In many cases, plunger 225will be fabricated predominantly from an elastomeric cover material. Ifthe side walls of plunger 225 do not make adequate sealing contact withthe interior side wall of syringe barrel 210, leakage of contrast to therear of plunger 225 can occur during advancement of plunger 225.

[0113] Although the present invention has been described in detail inconnection with the above examples, it is to be understood that suchdetail is solely for that purpose and that variations can be made bythose skilled in the art without departing from the spirit of theinvention except as it may be limited by the following claims.

What is claimed is:
 1. An adapter for releasably attaching a syringe toan injector, wherein the syringe comprises a body having a forward endand a rearward end, and a plunger slideably positioned within the body,and wherein the injector comprises a front wall, an opening formed inthe front wall, and a drive member reciprocally mounted in the injector,the adapter comprising: a syringe carrier adapted to seat at least aportion of the syringe, the syringe carrier comprising a front end, arear end and at least one rearward facing abutment member operable toabut at least a portion of a forward facing surface associated with thesyringe, the syringe carrier defining an opening therein to allow thedrive member of the injector to engage the plunger; a releasablemounting mechanism associated with the syringe carrier to mount theadapter in a desired position relative to the front wall of theinjector; and at least one syringe retaining mechanism for retaining thesyringe within the syringe carrier.
 2. The adapter of claim 1 whereinthe syringe further comprises a syringe neck associated with the forwardend of the body, the syringe neck and the body defining a transitionregion therebetween, the abutment member operable to abut a forwardfacing surface of the transition region.
 3. The adapter of claim 2wherein the abutment member abuts the transition region only in thevicinity of the transition from the forward end of the body to thesyringe neck.
 4. The adapter of claim 1 wherein the syringe furthercomprises a flange disposed on the rearward end of the body, theabutment member operable to abut the syringe flange.
 5. The adapter ofclaim 4 wherein the abutment member abuts the syringe flange only in thevicinity of the transition from the rearward end of the body to thesyringe flange.
 6. The adapter of claim 1 wherein at least a portion ofthe adapter is formed to enable viewing of the syringe.
 7. The adapterof claim 1 wherein the releasable mounting mechanism comprises one ormore flanges that cooperate with the injector to mount the adapter tothe injector.
 8. The adapter of claim 1 , further comprising a sealingflange positioned forward of the releasable mounting mechanism to abutthe front wall of the injector.
 9. The adapter of claim 1 , furthercomprising indicia for providing information to the injector.
 10. Theadapter of claim 1 , further comprising at least one syringe abutmentmember to prevent the syringe from rotating within the adapter.
 11. Theadapter of claim 1 wherein the syringe further comprises a handleattached to the plunger, the handle extending out of the rear of thesyringe body, the adapter further comprising a guide member to guide themovement of the handle of the syringe.
 12. The adapter of claim 1wherein the abutment member comprises a resilient material.
 13. Theadapter of claim 1 wherein the at least one syringe retaining mechanismis rotatable around an axis of the adapter between an open position anda closed position.
 14. The adapter of claim 1 wherein the at least onesyringe retaining mechanism is slidable along an axis of the adapter.15. The adapter of claim 1 wherein the at least one syringe retainingmechanism comprises at least one extending member that is biased in aposition to retain the syringe in the adapter.
 16. The adapter of claim1 wherein the at least one syringe retaining mechanism is hingedlyattached to one side of the adapter to be movable between an openposition and a closed position.
 17. The adapter of claim 1 wherein thereleasable mounting mechanism comprises a plate that is removablyattachable to the front wall of the injector.
 18. The adapter of claim 1wherein the drive member does not connectively engage the plunger. 19.The adapter of claim 1 wherein the releasable mounting mechanism isdisposed on the rearward end of the syringe carrier.
 20. The adapter ofclaim 1 , further comprising a push rod disposed within the opening inthe syringe carrier, the push rod comprising a distal end that isoperable to engage the plunger of the syringe and a proximal end that isoperable to engage the drive member of the injector.